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Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Director, Regulatory Affairs — CMC FSP

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree or equivalent and a relevant formal academic or vocational qualification are required.
  • Previous experience providing the knowledge, skills, and abilities to perform the job, comparable to 12 or more years, is required.
  • At least 5 years of management responsibility is required.
  • Superior English-language communication and negotiation skills, both oral and written, and local-language skills where applicable are required.
  • Advanced knowledge of CMC regulatory affairs, including relevant global, regional, and national requirements and procedures for clinical trial authorization, marketing authorization, and product lifecycle management, is required.
  • A superior understanding of ICH guidelines and other relevant global regulatory guidance, and the ability to apply CMC regulatory knowledge to client and project needs, is required.
  • The ability to provide practical CMC advice across client requests, ad hoc assignments, and cross-functional queries, and to recognize when escalation or additional expertise is needed, is required.
  • The ability to independently assess sponsor needs and work with project team members to produce compliant deliverables is required.
  • Advanced understanding of budgeting and forecasting, along with analytical, investigative, and detail-oriented skills, is required.
  • The ability to supervise, evaluate, mentor, and develop departmental personnel; delegate work; and facilitate timely completion of assignments is required.
  • The ability to provide functional oversight to FSP teams, balance competing priorities, and respond to changing client and business needs is required.
  • The ability to support business development by translating client requirements into clear CMC scope, delivery, and resource considerations is required.
  • The ability to drive innovation and develop ideas that improve processes, productivity, and service quality is required.
  • Organizational, judgment, analytical, decision-making, and interpersonal skills, including the ability to manage complex work in parallel, are required.
  • Computer skills, including Microsoft Word, Microsoft Excel, Adobe Acrobat, and related tools, are required.
  • The ability to learn new technologies independently and act effectively as a liaison with other departments is required.
  • A combination of appropriate education, training, and/or directly related experience may be considered sufficient to meet the role requirements in some cases.

Responsibilities

  • Lead, coach, and develop staff, including interviewing and selection, preparing job descriptions, professional development, goal setting, performance management, behavioral and technical coaching and mentoring, employee counseling, and separations.
  • Approve or recommend actions related to salary administration, hiring, corrective action, and termination.
  • Review and approve time records, expense reports, leave requests, and overtime.
  • Promote the company's Equal Employment Opportunity policy and Affirmative Action Plan, and ensure adherence to ethical and regulatory standards.
  • Provide CMC regulatory subject-matter expertise to internal and external clients by responding to requests, ad hoc assignments, and queries from other functions with clear, timely advice, and identify when additional expertise or escalation is needed.
  • Advise clients on CMC regulatory strategy and product development considerations across relevant development, registration, and lifecycle-management stages.
  • Provide project-specific technical expertise and coordination oversight, including for key client projects.
  • Serve as an executive contact for key clients on CMC-related matters and support client discussions, including regulatory authority meetings and other public-facing engagements, as appropriate.
  • Promote quality performance across key and managed projects.
  • Provide functional oversight and delivery support for CMC FSP teams by aligning team capabilities, work allocation, and delivery expectations with client requirements; monitor performance and address risks, quality concerns, or changing priorities in a timely manner.
  • Support resource planning and forecasting across CMC work by assessing capability and capacity needs, recommending resource allocations, and adjusting staffing plans in response to changes in scope, workload, or client priorities.
  • Oversee project budgeting and forecasting, including recommendations on resource shifts and allocations in response to changes in scope or personnel requirements, to maintain delivery within budget.
  • Lead and participate in project meetings.
  • Identify out-of-scope activities promptly and partner with relevant functions to assess impact, communicate with the client, and progress contract modifications.
  • Collaborate with business development and senior management to price and secure new CMC and FSP business.
  • Contribute CMC expertise to client presentations, proposals, bid text, budgets, and contract discussions through closure.
  • Pursue collaborative and standalone opportunities and support existing clients seeking additional services.
  • Partner with business development, operations, and functional leaders to assess prospective work, clarify CMC scope and delivery needs, and inform decisions on feasibility, team structure, and resourcing.
  • Contribute to the development and implementation of global and regional CMC functional plans.
  • Ensure compliance with relevant organizational and departmental SOPs and WPDs, and promote consistent application across CMC FSP teams.
  • Develop strategies and lead development and implementation of processes and procedures that improve team productivity, accuracy, and consistency.
  • Contribute to the development and implementation of systems and tools that improve efficiency across CMC activities.
  • Support process improvement, cycle-time reduction, submission activities, metrics, and other key performance indicators.

About the Company

Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Thermo Fisher Scientific makes and sells the instruments, chemicals, consumables and lab services that drug companies, hospitals, universities and industrial labs use for research, testing and production. Its products cover work from gene sequencing and protein analysis to diagnostic tests and lab freezers, and its distribution arm ships supplies to labs worldwide. Drug developers also hire it to run clinical trials and to manufacture medicines under contract. It earns money from consumables that labs buy again and again, along with instrument sales, service contracts and outsourcing fees. The company traces its roots to Thermo Electron, founded in 1956, which merged with Fisher Scientific in 2006, and it is based in Waltham, Massachusetts.

Company size
10,001+
Company stage
IPO
Headquarters
Waltham, MA
Founded
1956

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